Trial Capabilities & Site Activation Specialist

Eli Lilly and Company; Indianapolis (IN); On-site; USD 66,000 - 154,000; Full time

Job summary

Eli Lilly and Company is seeking a Trial Capabilities Senior Associate to ensure investigator sites meet enrollment requirements and support trial maintenance. You will manage regulatory documents, budgets, contracts, and Trial Master Files across clinical development in a fast-paced environment.

The role emphasizes collaboration with investigators and internal teams, ensuring inspection readiness and adherence to financial and legal guidelines, while maintaining a focus on patient safety and

Qualifications

• Bachelor’s degree preferably in a scientific or health related field.
• Two years clinical research experience or relevant experience preferred.
• Lean/Six Sigma background.
• Understanding of the overall clinical development paradigm and the importance of efficient site activation.

Responsibilities

• Initiate investigator activities, including collection and submission of regulatory documents and budgets.
• Communicate with investigators to enable start-up and ongoing collaboration.
• Identify, communicate, and resolve issues across trials.
• Ensure regulatory/data privacy requirements are incorporated into submissions.
• Populate Trial Master Files and related systems for accuracy.

Skills

Communication

Negotiation

Project management

Problem solving

Self-management

Organizational skills

Lean/Six Sigma

Language Capabilities

Education

Bachelor’s degree in scientific/health field

Job description

Eli Lilly and Company is seeking a Trial Capabilities Senior Associate to ensure investigator sites meet enrollment requirements and support trial maintenance. You will manage regulatory documents, budgets, contracts, and Trial Master Files across clinical development in a fast-paced environment.

The role emphasizes collaboration with investigators and internal teams, ensuring inspection readiness and adherence to financial and legal guidelines, while maintaining a focus on patient safety and